Reviewed,
UniProtKB/Swiss-Prot Q9UNA1 (RHG26_HUMAN)
Last modified
November 25, 2008.
Version 84.
History...
Clusters with 100%,
90%,
50% identity |
Documents (6) |
Third-party data |
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Names and origin
| Protein names | Recommended name: Rho GTPase-activating protein 26 Alternative name(s): Rho-type GTPase-activating protein 26 Oligophrenin-1-like protein GTPase regulator associated with focal adhesion kinase | ||||
| Gene names |
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| Organism | Homo sapiens (Human) | ||||
| Taxonomic identifier | 9606 [NCBI] | ||||
| Taxonomic lineage | Eukaryota › Metazoa › Chordata › Craniata › Vertebrata › Euteleostomi › Mammalia › Eutheria › Euarchontoglires › Primates › Haplorrhini › Catarrhini › Hominidae › Homo |
Protein attributes
| Sequence length | 814 AA. |
| Sequence status | Complete. |
| Sequence processing | The displayed sequence is not processed. |
| Protein existence | Evidence at protein level. |
General annotation (Comments)
| Function | GTPase-activating protein for RhoA. |
| Subunit structure | Binds to the C-terminal of pp125(FAK). |
| Involvement in disease | Defects in ARHGAP26 are a cause of juvenile myelomonocytic leukemia (JMML) [MIM:607785]. JMML is a pediatric myelodysplastic syndrome that constitutes approximately 30% of childhood cases of myelodysplastic syndrome (MDS) and 2% of leukemia. Chromosomal translocation t(5;11)(q31;q23) with MLL has been found in a JMML patient. |
| Sequence similarities | Contains 1 PH domain. Contains 1 Rho-GAP domain. Contains 1 SH3 domain. |
Ontologies
Keywords | |
|---|---|
| Coding sequence diversity | Alternative splicing Chromosomal rearrangement |
| Disease | Disease mutation Proto-oncogene |
| Domain | SH3 domain |
| Molecular function | GTPase activation |
| Technical term | 3D-structure |
Gene Ontology (GO) | |
| Biological process | actin cytoskeleton organization Non-traceable author statement. Source: UniProtKB nervous system developmentNon-traceable author statement. Source: UniProtKB signal transductionInferred from electronic annotation. Source: InterPro |
| Cellular component | intracellular Inferred from electronic annotation. Source: InterPro |
| Molecular function | Rho GTPase activator activity Ref.2 Non-traceable author statement. Source: UniProtKB protein bindingInferred from physical interaction. Source: IntAct |
| Complete GO annotation... | |
Alternative products
| This entry describes 2 isoforms produced by alternative splicing. [Align] [Select] | ||||||
| Isoform 1 (identifier: Q9UNA1-1) This isoform has been chosen as the 'canonical' sequence. All positional information in this entry refers to it. This is also the sequence that appears in the downloadable versions of the entry. | ||||||
| Isoform 2 (identifier: Q9UNA1-2) The sequence of this isoform differs from the canonical sequence as follows: 700-754: Missing. |
Sequence annotation (Features)
| Feature key | Position(s) | Length | Description | Graphical view | Feature identifier | ||||||||||||||||
Molecule processing | |||||||||||||||||||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| Chain | 1 – 814 | 814 | Rho GTPase-activating protein 26 | PRO_0000056718 | |||||||||||||||||
Regions | |||||||||||||||||||||
| Domain | 265 – 369 | 105 | PH | ||||||||||||||||||
| Domain | 383 – 568 | 186 | Rho-GAP | ||||||||||||||||||
| Domain | 756 – 814 | 59 | SH3 | ||||||||||||||||||
| Compositional bias | 584 – 701 | 118 | Ser-rich | ||||||||||||||||||
Natural variations | |||||||||||||||||||||
| Alternative sequence | 700 – 754 | 55 | Missing in isoform 2. | VSP_001659 | |||||||||||||||||
| Natural variant | 417 | 1 | N → S in JMML. | VAR_013623 | |||||||||||||||||
Experimental info | |||||||||||||||||||||
| Sequence conflict | 355 | 1 | E → G Ref.2 Ref.3 | ||||||||||||||||||
Secondary structure | |||||||||||||||||||||
Helix Strand Turn | |||||||||||||||||||||
| Beta strand | 761 – 765 | 5 | |||||||||||||||||||
| Beta strand | 771 – 774 | 4 | |||||||||||||||||||
| Beta strand | 782 – 785 | 4 | |||||||||||||||||||
| Beta strand | 794 – 801 | 8 | |||||||||||||||||||
| Beta strand | 803 – 807 | 5 | |||||||||||||||||||
| Helix | 808 – 810 | 3 | |||||||||||||||||||
| Beta strand | 811 – 813 | 3 | |||||||||||||||||||
Sequences
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References
| « Hide 'large scale' references | |
| [1] | "Molecular cloning of human oligophrenin-1 like (OPHN1L) gene, complete CDS." Xia J.H., Tang X.X., Yu K.P., Pan Q., Dai H.P. Submitted (APR-1999) to the EMBL/GenBank/DDBJ databases Cited for: NUCLEOTIDE SEQUENCE (ISOFORM 1). Tissue: Heart, Liver and Placenta. |
| [2] | "The human GRAF gene is fused to MLL in a unique t(5;11)(q31;q23) and both alleles are disrupted in three cases of myelodysplastic syndrome/acute myeloid leukemia with a deletion 5q." Borkhardt A., Bojesen S., Haas O.A., Fuchs U., Bartelheimer D., Loncarevic I.F., Bohle R.M., Harbott J., Repp R., Jaeger U., Viehmann S., Henn T., Korth P., Scharr D., Lampert F. Proc. Natl. Acad. Sci. U.S.A. 97:9168-9173(2000) [PubMed: 10908648] [Abstract] Cited for: NUCLEOTIDE SEQUENCE [GENOMIC DNA] (ISOFORM 2), DISEASE, VARIANT LEUKEMIA SER-417. |
| [3] | "Genomic structure of the human GRAF gene." Bojesen S.E., Link C., Borkhardt A. Submitted (JAN-2001) to the EMBL/GenBank/DDBJ databases Cited for: NUCLEOTIDE SEQUENCE OF 53-785 (ISOFORMS 1 AND 2). |
| [4] | "Prediction of the coding sequences of unidentified human genes. X. The complete sequences of 100 new cDNA clones from brain which can code for large proteins in vitro." Ishikawa K., Nagase T., Suyama M., Miyajima N., Tanaka A., Kotani H., Nomura N., Ohara O. DNA Res. 5:169-176(1998) [PubMed: 9734811] [Abstract] Cited for: NUCLEOTIDE SEQUENCE [LARGE SCALE MRNA] OF 62-814 (ISOFORM 1). Tissue: Brain. |
| [5] | "Solution structure of the SH3 domain of human oligophrenin-1-like protein (KIAA0621)." RIKEN structural genomics initiative (RSGI) Submitted (DEC-2003) to the PDB data bank Cited for: STRUCTURE BY NMR OF 754-814. |
| + | Additional computationally mapped references. |
Cross-references
Sequence databases | |||||||||||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| AF141884 mRNA. Translation: AAD39482.1. Y10388 Genomic DNA. Translation: CAA71414.2. AJ309466 AJ309487 Genomic DNA. Translation: CAC29145.2. AJ309466 AJ309487 Genomic DNA. Translation: CAC29146.2. AB014521 mRNA. Translation: BAA31596.1. | |||||||||||||
| PIR | F59430. | ||||||||||||
| RefSeq | NP_055886.1. | ||||||||||||
| UniGene | Hs.654668 | ||||||||||||
3D structure databases | |||||||||||||
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| ModBase | Search... | ||||||||||||
Protein-protein interaction databases | |||||||||||||
| IntAct | Q9UNA1. | ||||||||||||
PTM databases | |||||||||||||
| PhosphoSite | Q9UNA1. | ||||||||||||
Genome annotation databases | |||||||||||||
| Ensembl | ENSG00000145819. Homo sapiens. [Contig view] | ||||||||||||
| GeneID | 23092. | ||||||||||||
| KEGG | hsa:23092. | ||||||||||||
Organism-specific databases | |||||||||||||
| H-InvDB | HIX0005269. | ||||||||||||
| HGNC | HGNC:17073. ARHGAP26. | ||||||||||||
| MIM | 605370. gene. 607785. phenotype. | ||||||||||||
| PharmGKB | PA134946198. | ||||||||||||
| HUGE | Search... | ||||||||||||
| GenAtlas | Search... | ||||||||||||
| GeneCards | Search... | ||||||||||||
Phylogenomic databases | |||||||||||||
| HOGENOM | Q9UNA1. | ||||||||||||
| HOVERGEN | Q9UNA1. | ||||||||||||
Enzyme and pathway databases | |||||||||||||
| Reactome | REACT_11044. Signaling by Rho GTPases. | ||||||||||||
Gene expression databases | |||||||||||||
| ArrayExpress | Q9UNA1. | ||||||||||||
| CleanEx | HS_ARHGAP26. | ||||||||||||
| GermOnline | ENSG00000145819. Homo sapiens. | ||||||||||||
Family and domain databases | |||||||||||||
| InterPro | IPR001849. PH. IPR000198. RhoGAP. IPR001452. SH3. [Graphical view] | ||||||||||||
| Pfam | PF00169. PH. 1 hit. PF00620. RhoGAP. 1 hit. PF00018. SH3_1. 1 hit. [Graphical view] | ||||||||||||
| PRINTS | PR00452. SH3DOMAIN. | ||||||||||||
| ProDom | PD000066. SH3. 1 hit. [Graphical view] [Entries sharing at least one domain] | ||||||||||||
| SMART | SM00233. PH. 1 hit. SM00324. RhoGAP. 1 hit. SM00326. SH3. 1 hit. [Graphical view] | ||||||||||||
| PROSITE | PS50003. PH_DOMAIN. 1 hit. PS50238. RHOGAP. 1 hit. PS50002. SH3. 1 hit. [Graphical view] | ||||||||||||
| ProtoNet | Search... | ||||||||||||
Other Resources | |||||||||||||
| LinkHub | Q9UNA1. | ||||||||||||
| NextBio | 44247. | ||||||||||||
| SOURCE | Search... | ||||||||||||
Entry information
| Entry name | RHG26_HUMAN | ||||||||
| Accession | Primary (citable) accession number: Q9UNA1 Secondary accession number(s): O75117 Q9UJ00 | ||||||||
| Entry history |
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| Entry status | Reviewed (UniProtKB/Swiss-Prot) | ||||||||
| Annotation project | HPI (Human Proteome Initiative) | ||||||||
Relevant documents
| Human chromosome 5 Human chromosome 5: entries, gene names and cross-references to MIM |
| Human entries with polymorphisms or disease mutations List of human entries with polymorphisms or disease mutations |
| Human polymorphisms and disease mutations Index of human polymorphisms and disease mutations |
| MIM cross-references Online Mendelian Inheritance in Man (MIM) cross-references in UniProtKB/Swiss-Prot |
| PDB cross-references Index of Protein Data Bank (PDB) cross-references |
| SIMILARITY comments Index of protein domains and families |

Clusters with


